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SUCRALFATE

NDC 72189-234, SUCRALFATE, tablet, from DIRECT RX.

Product NDC
72189-234
Status
Listed
Labeler
DIRECT RX
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070848
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUCRALFATE1 g/1

Pharmacologic classes

Aluminum Complex [EPC]; Organometallic Compounds [CS]

Package NDCNDC-11Package
72189-234-207218902342020 TABLET in 1 BOTTLE (72189-234-20)
72189-234-907218902349090 TABLET in 1 BOTTLE (72189-234-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c50b5044-31ed-672a-e053-2995a90a49fc

Use it

Look up 72189-234 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-234. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.